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Series GSE98952 Query DataSets for GSE98952
Status Public on May 17, 2017
Title Transcriptome analysis of lysozyme treated S. gallolyticus subsp. gallolyticus [UCN34]
Platform organism Streptococcus gallolyticus subsp. gallolyticus
Sample organism Streptococcus gallolyticus UCN34
Experiment type Expression profiling by array
Summary Streptococcus gallolyticus subsp. gallolyticus is a commensal of the human gastrointestinal tract and a pathogen of infective endocarditis and other biofilm-associated infections with exposed collagen. Therefore, this study focuses on the characterization of the biofilm formation and collagen adhesion of S. gallolyticus subsp. gallolyticus under different conditions. It has been observed that lysozyme triggers biofilm formation divergently in the analyzed S. gallolyticus subsp. gallolyticus strains. The transcriptome analysis was performed for two strains which form more biofilm in the presence of lysozyme. Lysozyme leads to higher expression of genes of transcription and translation, of the dlt operon (cell wall modification), of hydrogen peroxide resistance proteins and of two immunity proteins which could be involved in biofilm formation. Furthermore, the adhesion ability of 73 different S. gallolyticus subsp. gallolyticus strains to collagen type I and IV was analyzed. High adhesion ability was observed for the strain UCN 34, whereas the strain DSM 16831 adhered only marginally to collagen. The full genome microarray analysis revealed strain-dependent gene expression due to adhesion. The expression of genes of a transposon and a phage region in strain DSM 16831 were increased, which corresponds to lateral gene transfer. Adherence to collagen leads to a change in the expression of genes of nutrients uptake in the strain UCN 34.
 
Overall design Analysis of two S. gallolyticus subsp. gallolyticus strains (BAA-2069 and UCN 34) in BHI medium with 10 mg/ml lysozyme compared to control (BHI medium without lysozym) after 5 hours of incubation. For each strain and condition three biological replicates were taken and normalized on the control without lysozyme.
 
Contributor(s) Grimm I, Vollmer T, Dreier J
Citation(s) 29373594
Submission date May 16, 2017
Last update date Jul 25, 2021
Contact name Imke Grimm
E-mail(s) [email protected]
Organization name Herz- und Diabeteszentrum NRW; Universitätsklinikum der Ruhr-Universität Bochum
Department Institut für Laboratoriums- und Transfusionsmedizin
Street address Georgstraße 11
City Bad Oeynhausen
ZIP/Postal code 32545
Country Germany
 
Platforms (1)
GPL23196 Agilent-072445 ArrayXS_S.gallolyticus_01-2015 [gene version]
Samples (6)
GSM2628261 UCN 34 a BHI
GSM2628262 UCN 34 a LYZ
GSM2628263 UCN 34 e BHI
This SubSeries is part of SuperSeries:
GSE98955 Transcriptome analysis of S. gallolyticus subsp. gallolyticus
Relations
BioProject PRJNA387069

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE98952_RAW.tar 5.7 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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